Assaying mitochondrial respiratory complex activity in mitochondria isolated from human cells and tissues.
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Uncoupling protein-4 (UCP4) increases ATP supply by interacting with mitochondrial Complex II in neuroblastoma cellsCardiolipin switch in mitochondria: shutting off the reduction of cytochrome C and turning on the peroxidase activityRespiratory complex III is required to maintain complex I in mammalian mitochondriaMitochondrial lipid abnormality and electron transport chain impairment in mice lacking alpha-synucleinCardiolipin and electron transport chain abnormalities in mouse brain tumor mitochondria: lipidomic evidence supporting the Warburg theory of cancerTyk2 tyrosine kinase expression is required for the maintenance of mitochondrial respiration in primary pro-B lymphocytesTruncated product of the bifunctional DLST gene involved in biogenesis of the respiratory chainIncreased learning and brain long-term potentiation in aged mice lacking DNA polymerase μRadiation-induced signaling results in mitochondrial impairment in mouse heart at 4 weeks after exposure to X-raysRetained features of embryonic metabolism in the adult MRL mouseProtective mechanisms of mitochondria and heart function in diabetesImplications of altered glutathione metabolism in aspirin-induced oxidative stress and mitochondrial dysfunction in HepG2 cellsA phosphodiesterase 2A isoform localized to mitochondria regulates respirationNAC attenuates LPS-induced toxicity in aspirin-sensitized mouse macrophages via suppression of oxidative stress and mitochondrial dysfunctionAlteration of renal respiratory Complex-III during experimental type-1 diabetesThe mitochondrial SDHD gene is required for early embryogenesis, and its partial deficiency results in persistent carotid body glomus cell activation with full responsiveness to hypoxiaThe mitochondrial disease associated protein Ndufaf2 is dispensable for Complex-1 assembly but critical for the regulation of oxidative stressAssessment of ToxCast Phase II for Mitochondrial Liabilities Using a High-Throughput Respirometric AssayMitochondrial oxidative stress and epilepsy in SOD2 deficient mice: attenuation by a lipophilic metalloporphyrin.Optical spectroscopy in turbid media using an integrating sphere: mitochondrial chromophore analysis during metabolic transitions.Data mining of NCI's anticancer screening database reveals mitochondrial complex I inhibitors cytotoxic to leukemia cell lines.Mitochondrial mechanism of neuroprotection by CARTMitochondrial membrane potential in human neutrophils is maintained by complex III activity in the absence of supercomplex organisationEnhancement of L-3-hydroxybutyryl-CoA dehydrogenase activity and circulating ketone body levels by pantethine. Relevance to dopaminergic injury.Metabolic changes and inflammation in cultured astrocytes from the 5xFAD mouse model of Alzheimer's disease: Alleviation by pantethine.Novel role of ATPase subunit C targeting peptides beyond mitochondrial protein import.Deficiency of electron transport chain in human skeletal muscle mitochondria in type 2 diabetes mellitus and obesity.Increased mitochondrial matrix-directed superoxide production by fatty acid hydroperoxides in skeletal muscle mitochondria.Control of oxidative phosphorylation by vitamin A illuminates a fundamental role in mitochondrial energy homoeostasis.Modulation of mitochondrial protein phosphorylation by soluble adenylyl cyclase ameliorates cytochrome oxidase defects.Nitration of the mitochondrial complex I subunit NDUFB8 elicits RIP1- and RIP3-mediated necrosisA switch in the source of ATP production and a loss in capacity to perform glycolysis are hallmarks of hepatocyte failure in advance liver disease.Mutant TDP-43 does not impair mitochondrial bioenergetics in vitro and in vivoMolecular and biochemical characterisation of a novel mutation in POLG associated with Alpers syndrome.Evolution meets disease: penetrance and functional epistasis of mitochondrial tRNA mutations.The CREB/CRE transcriptional pathway: protection against oxidative stress-mediated neuronal cell deathDicarboxylate carrier-mediated glutathione transport is essential for reactive oxygen species homeostasis and normal respiration in rat brain mitochondria.Inhibition of human peptide deformylase disrupts mitochondrial functionPost-translational oxidative modification and inactivation of mitochondrial complex I in epileptogenesisA role for human mitochondrial complex II in the production of reactive oxygen species in human skin
P2860
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P2860
Assaying mitochondrial respiratory complex activity in mitochondria isolated from human cells and tissues.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh
2001年學術文章
@zh-hant
name
Assaying mitochondrial respira ...... from human cells and tissues.
@en
Assaying mitochondrial respira ...... from human cells and tissues.
@nl
type
label
Assaying mitochondrial respira ...... from human cells and tissues.
@en
Assaying mitochondrial respira ...... from human cells and tissues.
@nl
prefLabel
Assaying mitochondrial respira ...... from human cells and tissues.
@en
Assaying mitochondrial respira ...... from human cells and tissues.
@nl
P1476
Assaying mitochondrial respira ...... d from human cells and tissues
@en
P2093
D M Turnbull
M A Birch-Machin
P304
P356
10.1016/S0091-679X(01)65006-4
P577
2001-01-01T00:00:00Z